ClinVar Miner

List of variants in gene VCL reported as likely benign by Illumina Clinical Services Laboratory,Illumina

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 11
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HGVS dbSNP
NM_003373.4(VCL):c.*990_*991dup rs397804906
NM_014000.2(VCL):c.*1203A>C rs149551128
NM_014000.2(VCL):c.*292G>C rs77295081
NM_014000.3(VCL):c.*107T>A
NM_014000.3(VCL):c.*1636C>T
NM_014000.3(VCL):c.1542C>T (p.Val514=) rs7904077
NM_014000.3(VCL):c.1671C>T (p.Asp557=) rs137877092
NM_014000.3(VCL):c.2521G>C (p.Asp841His) rs150385900
NM_014000.3(VCL):c.2801C>T (p.Ala934Val) rs16931179
NM_014000.3(VCL):c.660C>T (p.Asn220=) rs56264452
NM_014000.3(VCL):c.945C>A (p.Gly315=) rs61731180

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